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4th International Conference on Clinical Trials

Organizer: Christopher Bradley

4th International Conference on Clinical Trials

Event Opening Date:  11. September 2017

Event Termination Date:  13. September 2017

San Antonio, Texas, USA

An Insight into Innovative Approaches in Global Clinical Research and Clinical Trials

After a Successful conference in 2016, we are bringing forth "4th International Conference on Clinical Trials" (Clinical Trials 2017) during September 11-13, 2017 at San Antonio, USA, with the main theme as “An Insight into Innovative Approaches in Global Clinical Research and Clinical Trials”. The conference invites all the participants across the globe to attend and share their insights and convey recent developments in the field of Clinical Research and Trials.

Clinical Trials 2017 anticipates large number of participants from all over the world with thought provoking Keynote lectures, Plenary speeches, Workshops, Symposiums, Poster presentations, Special sessions and Career development programs. The conference provides the perfect platform for the scientific community as an interactive and engaging 3-day event: unique in format, content, networking and engagement. This event aims at by bringing together clinical research, clinical trials, medical and pharma professionals; Academicians, doctors, CRO’s, CMO’s, study sponsors, related associations & societies; Executives from biomedical, biotech, biophrma, medical devices and pharmaceutical industries around the globe to discuss innovations and advancements in this exciting field.

Conference Tracks/Sessions: Clinical Trials 2017 includes 20 Tracks/Sessions and 80+ Sub-Tracks which covers all the aspects starting from Drug discovery, Pre-clinical research to Post marketing clinical trials.

  • Drug Discovery and Development
  • Clinical Research & Clinical Trials
  • Clinical Study Designs
  • Conducts of Clinical Trials
  • Patient-Centric Clinical Trials
  • Research and Trials on AIDS / Cancer / Diabetes
  • Clinical Trials on different Diseases
  • Clinical Data Management and Statistics
  • Globalization of Clinical Trials
  • Innovations in Clinical Trials
  • Future of Clinical Trials
  • CRO/Sponsorship Clinical Trials
  • Clinical Trial Site Management and Business Development
  • Outsourcing in Clinical Trials
  • Bioethics and Quality Regulation
  • Clinical and Medical Case Reports
  • Pharmacovigilance and Drug Safety
  • Post-marketing Surveillance and many more…

2017 Highlights:

  • 300+ Participation (70% Industry: 30% Academia)
  • 5+ Keynote Speakers
  • 50+ Plenary Speakers
  • 20+ Exhibitors
  • 14 Innovative Educational Sessions
  • 5+ Workshops
  • B2B Meetings

Organizing Committee Members:

  • Clayton A. Dehn, Clinical Trials of Texas, USA
  • Oleg V. Tcheremissine, Carolinas Healthcare System, USA
  • Nicki Norris, Symphony Clinical Research, USA
  • Joao Paulo Tardivo, Faculty of Medicine of ABC, Brazil
  • Paul Michael Ramirez, CNS Ratings LLC, USA
  • Entsuah Anthony Richard, Merck & Co., Inc., USA
  • David M Vulcano, Hospital Corporation of America, USA
  • Katarzyna Anna Rygiel, Silesian University School of Medicine, Poland
  • Scott Gelfand, Oklahoma State University, USA
  • JoAnn Pfeiffer, Arizona State University, USA

Benefits of Attending Clinical Trials 2017:

  • Certificate Accreditation by the International Organizing Committee
  • Abstracts will be published in conference souvenirs & Related International Journals, provided with DOI by cross reference
  • Live Streaming of your presentation through our websites and YouTube (up on your interest)
  • Speaker and Abstract pages created in Google on your name and title of your talk/presentation would get worldwide acknowledgment to your profile and Research
  • An opportunity to launch your Book/Chapter/Research work at the event
  • Promotion for your own labs will be feasible
  • Opportunity to conduct a workshop/symposium
  • Special interactive sessions will be provided to your research team
  • Pre-Conference and Post-Conference Networking with Experts in the field
  • B2B meetings/Scientific networking for Research collaborations

Who You’ll Meet?

Directors/Senior Directors/Executive Directors and Vice Presidents/Senior Vice Presidents/Executive Vice Presidents and Heads/Leaders/Partners of

  • CROs and CMOs
  • Clinical Research Sites
  • Pharma/Biotech and Medical Device industries
  • Hospitals, Associations

Medical Directors, Principal Investigators, Methodologists, and other clinical research professionals along with Academicians: University Faculties like Directors, Senior Professors/Assistant Professors/ Associate Professor, Research Scholars, scientists who are related to clinical and medical research. Clinical/Pharmaceutical and biotech industry professionals with responsibilities in:

  • Clinical Research & Development
  • Clinical Design/ Protocol Design/ Clinical Strategy
  • Global Clinical Operations/ Clinical Outsourcing
  • Biostatistics/Data management
  • Patient Recruitment/Enrollment
  • Clinical Trial Management/Clinical Trial Supplies
  • Regulatory Affairs

Why you should attend?

  • Get to the heart of Conducts of Clinical Research.
  • Dissect the challenges before looking for concrete solutions.
  • Discover how advances in the sector are impacting both large and small trials.
  • Explore tried and tested routes to improve positive results in trials.
  • Understand how to develop the right protocol, formulation and delivery strategy with a strong scientific, clinical and commercial mind set.
  • Discover the latest innovations in drug research and clinical trials.
  • Be inspired by innovative case studies and realize the potential impact on your clinical research processes.
  • Engage in the exciting event format, with round tables, panels, showcases, speed networking and multiple conference tracks.
  • Share experiences, insights and strategies in interactive peer-to peer round tables.
  • Hear more perspectives in one place – from large medium and small organizations from pharma, biotech, biopharma and academia.
  • Discover how clinical trial advancements are being implemented in practice.

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